Eficiência de fungicidas sistêmicos no controle da ferrugem do Eucalyptus

Avaliaram-se os efeitos curativo e protetor e o tempo de absorção de fungicidas sistêmicos no controle da ferrugem do eucalipto. Azoxyztrobin, triadimenol, tetraconazole, tebuconazole e epoxiconazole + pyraclostrobin apresentaram 100% de ação curativa quando aplicados até quatro dias após a inoculação. Aplicados após sete dias, apenas azoxystrobin, tebuconazole e epoxiconazole + pyraclostrobin mantiveram o efeito curativo. Aos 10 dias depois da inoculação, os fungicidas reduziram a infecção, mas não controlaram totalmente a doença. Além do efeito curativo, azoxystrobin e triadimenol proporcionaram efeito protetor quando aplicados até 21 dias antes da inoculação de P. psidii. Avaliou-se o tempo mínimo de absorção de azoxystrobin, tebuconazole, triadimenol e trifloxystrobin. Esses quatro fungicidas foram absorvidos pela planta em todos os intervalos testados - 30, 60, 90 e 120 min - e inibiram a infecção de P. psidii em mudas de eucalipto.

Efeitos do paclobutrazol no crescimento e na floração de crisântemo (Chrysanthemum moriflorum, Ramat)

Estudaram-se os efeitos de concentrações de paclobutrazol [(2 RS, 3 RS)-1-(4-clorofenil)-4,4-dimetil-2,1,2,4-triazol-1-il-) pentan-3-ol} sobre o crescimento e folração de crisântemo Puritain, cultivado em casa de vegetação com condições controlados de luz, temperatura e umidade relativa do ar. Empregou-se o delineamento estatístico de blocos ao acaso com 10 tratamentos repetidos cinco vezes, sendo cada repetição constituída de quatro vazos contendo cada um seis plants. Os tratamentos constaram de pulverização foliar única de paclobutrazol nas concentrações de 30, 45, 60, 75 e 90 ppm efetuados aos 21 dias após o plantio e de duas pulverizações efetuadas aos 17 e 28 dias após o plantio, nas concentrações de 15, 22,5 e 30 ppm cada. Como tratamento convencional usou-se o daminozine a 1300 ppm aplicado também em pulverização foliar aos 21 dias após o plantio; e foi mantida ainda uma testemunha sem tratamento. Os dados obtidos permitiram concluir que o paclobutrazol em todas as concentrações empregadas causou redução significativa na altura da plantas e essa redução foi crescente com o aumento da concentração. Os melhores resultados foram obtidos com concentrações de até 45 ppm aplicado em uma única vez e com daminozine a 1300 ppm, onde as alturas das plantas foram reduzidas a níveis ideais para comercialização, sem afetar a abertura dos botões florais. Duas aplicações de paclobutrazol nas concentrações de 22,5 ppm ou superiores e aplicações de 60 ppm ou superiores, reduziram excessivamente a altura das plantas e retardaram significativamente a abertura dos botões florais. Nenhuma das concentrações empregadas causou fitotoxicidade às plantas.

Dopaminergic profile of new heterocyclic N-phenylpiperazine derivatives

Dopamine constitutes about 80% of the content of central catecholamines and has a crucial role in the etiology of several neuropsychiatric disorders, including Parkinson's disease, depression and schizophrenia. Several dopaminergic drugs are used to treat these pathologies, but many problems are attributed to these therapies. Within this context, the search for new more efficient dopaminergic agents with less adverse effects represents a vast research field. The aim of the present study was to report the structural design of two N-phenylpiperazine derivatives, compound 4: 1-[1-(4-chlorophenyl)-1H-4-pyrazolylmethyl]-4-phenylhexahydropyrazine and compound 5: 1-[1-(4-chlorophenyl)-1H-1,2,3-triazol-4-ylmethyl]-4-phenylhexahydropyrazine, planned to be dopamine ligands, and their dopaminergic action profile. The two compounds were assayed (dose range of 15-40 mg/kg) in three experimental models: 1) blockade of amphetamine (30 mg/kg, ip)-induced stereotypy in rats; 2) the catalepsy test in mice, and 3) apomorphine (1 mg/kg, ip)-induced hypothermia in mice. Both derivatives induced cataleptic behavior (40 mg/kg, ip) and a hypothermic response (30 mg/kg, ip) which was not prevented by haloperidol (0.5 mg/kg, ip). Compound 5 (30 mg/kg, ip) also presented a synergistic hypothermic effect with apomorphine (1 mg/kg, ip). Only compound 4 (30 mg/kg, ip) significantly blocked the amphetamine-induced stereotypy in rats. The N-phenylpiperazine derivatives 4 and 5 seem to have a peculiar profile of action on dopaminergic functions. On the basis of the results of catalepsy and amphetamine-induced stereotypy, the compounds demonstrated an inhibitory effect on dopaminergic behaviors. However, their hypothermic effect is compatible with the stimulation of dopaminergic function which seems not to be mediated by D2/D3 receptors.

The Smiles rearrangement in hydrazidic systems and related syntheses /|nG. A. Pawelchak. -- 260 St. Catharines, Ont. : [s. n.],

This research was directed towards the investigation of the Smiles rearrangement in hydrazidic systems and the synthesis of related heterocyclic compounds. The work can be conveniently divided into two main sections. Section 1 of the thesis relates to the synthesis and examination of the O+N migration of phenoxy- derivatives of hydrazidic halides. In general, hydrazidic halides were found to react with 2-nitrophenol and 4-nitrophenol to give corresponding a-nitrophenoxy- compounds. These a-nitrophenoxy- compounds were found to rearrange in warm base to give the corresponding N-benzoyl compounds via a proposed five-membered transition state. Experiments conducted in styrene revealed no radical contribution to the rearrangement. Cross-over product analysis indicated the rearrangement as intramolecular and consistent with the Smiles rearrangement. The preparation of N-a-chlorobenzylidene-N'-2-nitrophenyl- -N'-(2,4-dibromophenyl)hydrazine from N-benzoyl-N'-2-nitrophenyl- N'-(2,4-dibromophenyl)hydrazine was accomplished using phosphorus oxychloride. Examination of this hydrazidic chloride indicated a marked decrease .in reactivity as compared to the N-a-chlorobenzylidene-N'-phenylhydrazine case. Section 2 concerns itself with the preparation of heterocyclic compounds using an analogy of the five-membered transition state present in the Smiles rearrangement of a substituted benzylidene derivatives A new preparation of 2,4-phenyl1,3,4- oxadiazol-S-one using N-benzoyl-N'-phenylhydrazine and ethyl thiochloroformate is reported. Two new preparations of N-a-thiobenzoyl-N'-(2,4-dibromophenylhydrazine are reported using sodium hydrosulfide in conjunction with N-a-bromobenzylidene-N'-(2,4-dibromophenyl)hydrazine in the first, and phosphorus pentasulfide with N-benzoylN'-( 2,4-dibromophenyl)hydrazine in the second. The latter is preferred due to the formation of a sulfide co-product in the former. Two preparations of 2-phenyl-4-(2,4-dibromophenyl)-1,3,4- thiadiazol-S-one are reported using N-thiobenzoyl-N'-(2,4-dibromophenyl) hydrazine and ethyl chloroformate and ethyl thiochloroformate Two rapid and easy preparations of 2-phenyl-4-(2,4-dibromophenyl)- 1,3,4-triazol-S-one are reported using ethyl chloroformate and ethyl thiochloroformate. Sodium cyanate in conjunction with a-aminobenzylidene-N'-(2,4-dibromophenyl)hydrazine also provided 2-phenyl-4-(2,4-dibromophenyl)-1,3,4-triazol-S-one Section 2 concludes with an examination of two possible mechanistic routes to the prepared heterocycles.

Coordenação entre as respostas da catalase e da ascorbato peroxidade em folhas de feijão caupi submetidas a diferentes fontes de peróxido de hidrogênio

The plants are often exposed to variations in environmental conditions that may trigger metabolic disturbances leading to a consequent loss in productivity of crops. These stressful conditions usually induce an accumulation of reactive oxygen species (ROS) in the cell, a condition known how oxidative stress. Among these species, hydrogen peroxide (H2O2) is an important molecule involved in numerous signaling mechanisms. The present study aimed to understand the relationship between the different enzymatic mechanisms of elimination of H2O2 by catalase (CAT) and ascorbate peroxidase (APX) in leaf tissues of seedlings of the species Vigna unguiculata L. Walp, under conditions of oxidative stress induced by application of CAT inhibitor, 3-amino-1,2,4-triazole (3-AT), and H2O2 itself on the roots. Three experiments were conducted. The first experiment was performed applying the compound 3-AT (5 mM) during the time (hours). In the second experiment, seedlings were exposed to different concentrations of H2O2 (2.5, 5.0, 7.5, 10 mM) for 48 h. The third strategy included the pre-treatment with H2O2 (2.5 mM) for 24 h, followed by subsequent treatment with the inhibitor 3-AT and recovery control condition. Treatment with 3-AT causes a strong inhibition of CAT activity in leaf tissues accompanied by an increase of activity of APX. However a decrease in oxidative damage to lipids is not observed as indicated by TBARS. It was observed that activity of APX is directly linked to the content of peroxide. Inductions in the activities of CAT and APX were observed mainly in the seedlings treated with 2.5 mM H2O2. This can be associated with a decrease in oxidative damage to lipids. In contrast, one same tendency was not observed in treatments with higher concentrations of this ROS. These results suggest that the concentration of 2.5 mM H2O2 can induce responses antioxidants later in seedling cowpea. This concentration when applied as pre-treatment for 24 h promoted an induction systems removers CAT and APX, both in activity and in terms of gene expression. However this increment was not observed in the recovered plants and the plants subsequently subjected to 3-AT. Additionally, the pretreatment was not sufficient to attenuate the inhibition of CAT activity and oxidative damage to lipids caused by the subsequent application of this inhibitor. The results showed that the application of 3-AT and H2O2 in the root systems of seedlings of cowpea promote changes in the parameters analyzed in leaf tissues that indicate a direct response to the presence of these factors or systemic signaling mecanisms. H2O2 appears to activate the responses of two antioxidant systems in this study thar does not promote greater protection in case of additional treatment with 3-AT. This demonstrates the importance of the CAT system. In this work, complete results indicate that there is a difference between the signaling and the effects caused by exposure to H2O2 and by treatment with 3-AT

Eficiência e viabilidade econômica do controle químico da ferrugem do eucalipto em condições de campo

Originária da América do Sul, a ferrugem do eucalipto causada pelo fungo Puccinia psidii, vem se tornando uma doença limitante para a cultura do eucalipto no Brasil, exigindo a adoção de estratégias de controle, dentre as quais está o controle químico. Para avaliar eficiência e viabilidade econômica de fungicidas no controle da ferrugem do eucalipto, montou-se um ensaio a campo. Para a instalação do ensaio, utilizou-se o delineamento em blocos ao acaso, em esquema fatorial 3 x 3 (3 produtos e 3 doses), sendo 0,5, 1,0 e 1,5 mL ou g do produto comercial por litro de solução. Os tratamentos foram: 1-) Testemunha; 2-) Fungicida azoxistrobina (estrobilurina); 3-) Fungicida tebuconazol (triazol); 4-) Fungicida tebuconazol + trifloxistrobina (triazol + estrobilurina). O experimento constou de quatro repetições, com avaliação da severidade das plantas. As avaliações foram efetuadas com base no percentual de área foliar lesionada. Verificou-se que com o aumento na dosagem dos fungicidas, houve maior redução da doença nas plantas aos 7 e 15 dias pós-aplicação. O fungicida tebuconazol + trifloxistrobina a 1,5 mL/L foi o mais eficiente contra a ferrugem do eucalipto em condições de campo. O fungicida tebuconazol apresentou maior viabilidade econômica nas três doses testadas.

Review of Fluconazole Properties and Analytical Methods for Its Determination

Fluconazole, alpha-(2.4-diflurofenil)-alpha-(1H-triazol-1-methyl)-1H-1,2,4-triazol-1-ethanol, is an antifungal of the triazoles class. It shows activity against species of Candida sp. and it is indicated in cases of oropharyngeal candidiasis, esophageal, vaginal, and deep infection. Fluconazole is a selective inhibitor of ergosterol, a steroid exclusive of the cell membrane of fungal cells. Fluconazole is highly absorbed by the gastrointestinal tract and spreads easily by body fluids. The main adverse reactions related to the use of fluconazole are nausea, vomiting, headache, rash, abdominal pain, diarrhea, and alopecia in patients undergoing prolonged treatment with a dose of 400 mg/day. In the form of raw material, pharmaceutical formulations, or biological material, fluconazole can be determined by methods such as titration, spectrophotometry, and thin-layer, gas, and liquid chromatography. This article discusses the pharmacological and physicochemical properties of fluconazole and also the methods of analysis applied to the determination of the drug.

Review of Fluconazole Properties and Analytical Methods for Its Determination

Fluconazole, -(2.4-diflurofenil)--(1H-triazol-1-methyl)-1H-1,2,4-triazol-1-ethanol, is an antifungal of triazoles class. It shows activity against species of Candida sp., and it is indicated in cases of oropharyngeal candidiasis, esophageal, vaginal, and deep infection. Fluconazole is a selective inhibitor of ergosterol, a steroid exclusive of the cell membrane of fungal cells. Fluconazole is highly absorbed by the gastrointestinal tract, and it spreads easily by body fluids. The main adverse reactions related to the use of fluconazole are nausea, vomiting, headache, rash, abdominal pain, diarrhea, and alopecia in patients undergoing prolonged treatment with a dose of 400 mg/day. In the form of raw material, pharmaceutical formulations, or biological material, fluconazole can be determined by methods such as titration, spectrophotometry, and thin-layer, gas, and liquid chromatography. This article discusses the pharmacological and physical-chemical properties of fluconazole and also the methods of analysis applied to the determination of the drug.

Assistência de ar e aplicação em volume baixo no controle da ferrugem asiática da soja (Phakopsora pachyrhizi Sydon & Sydon

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Propriedades analíticas e eletroanalíticas de um silsesquioxano nanoestruturado organofuncionalizado

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Ferrugem do eucalipto: Planejamento evasivo, estimativa de dano e análise da viabilidade do controle químico

Pós-graduação em Agronomia (Proteção de Plantas) - FCA

Complexos triazólicos de Pd(II): síntese, caracterização e atividade biológica

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

População de plantas e uso de piraclostrobina na cultura do milho: alterações agronômicas e fisiológicas

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Estudo de materiais nanoestruturados baseados em silsesquioxanos organomodificados: síntese, caracterização, formação de complexos e sorção de íons metálicos

Pós-graduação em Ciência e Tecnologia de Materiais - FC

Assistência de ar em barra, ângulo e volume de pulverização no controle de doenças e na produtividade da cultura do trigo

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)